A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517041



Internal ID20890402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:55421001..55422500hg38UCSC Ensembl
chr17:53498362..53499861hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182354
Samples
Known GenesMMD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517041
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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